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Inherited Creutzfeldt-Jakob disease

MONDO:0007403

Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.

Also known as: Creutzfeldt-Jakob disease, variant, resistance to, hereditary Creutzfeldt Jacob disease, inherited CJD, CJD, Creutzfeldt-Jakob disease, Creutzfeldt-Jakob disease, Heidenhain variant, Creutzfeldt-Jakob disease, familial, Creutzfeldt-Jakob disease, sporadic

17 clinical trials for this condition and its sub-types, 5 tagged with Inherited Creutzfeldt-Jakob disease itself.

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